Footprint Medical, Inc.

Footprint Medical, Inc. — FDA 510(k) Submissions

Footprint Medical, Inc. has submitted 4 FDA 510(k) premarket notifications since 2009, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days, Tubes, Gastrointestinal (and Accessories), Catheter, Umbilical Artery . Use the specialty filter in the sidebar to narrow results.